Crypthecodinium cohnii Growth and Omega Fatty Acid Production in Mediums Supplemented with Extract from Recycled Biomass

Crypthecodinium cohnii is a marine heterotrophic dinoflagellate that can accumulate high amounts of omega-3 polyunsaturated fatty acids (PUFAs), and thus has the potential to replace conventional PUFAs production with eco-friendlier technology. So far, C. cohnii cultivation has been mainly carried out with the use of yeast extract (YE) as a nitrogen source. In the present study, alternative carbon and nitrogen sources were studied: the extraction ethanol (EE), remaining after lipid extraction, as a carbon source, and dinoflagellate extract (DE) from recycled algae biomass C. cohnii as a source of carbon, nitrogen, and vitamins. In mediums with glucose and DE, the highest specific biomass growth rate reached a maximum of 1.012 h−1, while the biomass yield from substrate reached 0.601 g·g−1. EE as the carbon source, in comparison to pure ethanol, showed good results in terms of stimulating the biomass growth rate (an 18.5% increase in specific biomass growth rate was observed). DE supplement to the EE-based mediums promoted both the biomass growth (the specific growth rate reached 0.701 h−1) and yield from the substrate (0.234 g·g−1). The FTIR spectroscopy data showed that mediums supplemented with EE or DE promoted the accumulation of PUFAs/docosahexaenoic acid (DHA), when compared to mediums containing glucose and commercial YE.

Chlorophylls Extraction from Spinach Leaves Using Aqueous Solutions of Surface-Active Ionic Liquids

Chlorophylls and their derivatives have been extensively studied due to their unique and valuable properties, including their anti-mutagenic and anti-carcinogenic features. Nevertheless, high-purity-level chlorophylls extracted from natural sources are quite expensive because the methods used for their extraction have low selectivity and result in low yields. This study aimed to develop a “greener” and cost-effective technology for the extraction of chlorophylls from biomass using aqueous solutions of ionic liquids (ILs). Several aqueous solutions of ILs, with hydrotropic and surface-active effects were evaluated, demonstrating that aqueous solutions of surface-active ILs are enhanced solvents for the extraction of chlorophylls from spinach leaves. Operating conditions, such as the IL concentration and solid–liquid ratio, were optimized by a response surface methodology. Outstanding extraction yields (0.104 and 0.022 wt.% for chlorophyll a and b, respectively, obtained simultaneously) and selectivity (chlorophyll a/b ratio of 4.79) were obtained with aqueous solutions of hexadecylpyridinium chloride ([C16py]Cl) at moderate conditions of temperature and time. These extraction yields are similar to those obtained with pure ethanol. However, the chlorophyll a/b ratio achieved with the IL aqueous solution is higher than with pure ethanol (3.92), reinforcing the higher selectivity afforded by IL aqueous solutions as viable replacements to volatile organic compounds and allowing the obtainment of more pure compounds. Finally, the recovery and reuse of the solvent were evaluated by using a back-extraction step of chlorophylls using ethyl acetate. The results disclosed here bring new perspectives into the design of new approaches for the selective extraction of chlorophylls from biomass using aqueous solutions of surface-active ILs.

Determination of Methanol Concentration in Ethanol in Liquid Phase by a Phononic Crystal Mach-Zehnder Interferometer

A practical and portable ultrasonic interferometric sensor to detect methanol concentration in ethanol in the liquid phase is numerically investigated. For high-sensitivity operation, the sensor is designed as a Mach-Zehnder interferometer based on a linear-defect waveguide in a two-dimensional phononic crystal, which consists of square array of cylindrical steel rods in water. The waveguide core comprises polyethylene tubing, impedance-matched with water, filled with either pure ethanol or ethanol-methanol binary mixture, allowing fast replacement of the analyte. Band structure analyses through the finite-element method are carried out to obtain guiding modes at frequencies around 200 kHz. With 50x21 cells with 4.2 mm periodicity, the total sensor area is 210-by-88.2 millimeters, which can be significantly reduced by increasing the operating frequency to megahertz range. The interferometer is constructed via T junctions of the waveguide, which facilitates low-loss equal splitting and recollection of ultrasonic waves. Sample and reference wave paths are constructed by filling polyethylene tubing on the upper and lower halves of the interferometer with the ethanol-methanol mixture and pure ethanol, respectively. Frequency-domain finite-element method simulations reveal that the sensor output is characterized by several transmission peaks, one of which is centered at 203.35 kHz with a full-width at half-maximum of 20 Hz, resulting in a quality factor of 10167. The peak frequency of this peak redshifts at a rate of 7.24 Hz per percent volume fraction change in methanol. The peak shift is linear when the methanol volume fraction is below 10%. Besides, the interferometric sensor has a figure of merit around 0.35. The proposed ultrasonic sensor offers rapid detection of methanol content in ethanol with high sensitivity.

Performance, combustion, and emission evaluation of ethanol-gasoline blends ignited by diesel in dual-fuel intelligent charge compression ignition (ICCI) engine

A recent proposed dual-fuel combustion mode, intelligent charge compression ignition (ICCI), realizes the high-efficiency and clean combustion by organizing continuous stratification in a wide range of engine load. The paper investigated the performance of alcohol blended gasoline as low reactivity fuel (LRF) in ICCI combustion mode. Pure ethanol named E100 was also tested as LRF for comparison. To emphasize the differences of LRF properties and exclude the effect of the heat release phasing, the diesel injection timing was adjusted to maintain the same combustion phasing (CA50) at various LRF ratios under medium load. The results showed that E100 and E85 (ethanol ratio in gasoline-ethanol blend) promoted the degree of homogeneous combustion and eradicated soot emissions despite a slight increase of NOx. The maximum indicated thermal efficiency (ITE) was over 51.1% using E85, followed by 50.5% of E50. The perfect substitution ratio at the maximum ITE decreased from more than 80% to about 65% when increasing the ethanol ratio in LRF from 10% to 100%. The unregulated emissions such as aldehydes, ethylene, and methane, produced from incomplete combustion of ethanol were inhabited by E85, while the formation of toluene attributed to the appropriate carbon chain length of gasoline diminished when using E85 and E100.

Radiologic-pathologic analysis of increased ethanol localization and ablative extent achieved by ethyl cellulose

Ethanol provides a rapid, low-cost ablative solution for liver tumors with a small technological footprint but suffers from uncontrolled diffusion in target tissue, limiting treatment precision and accuracy. Incorporating the gel-forming polymer ethyl cellulose to ethanol localizes the distribution. The purpose of this study was to establish a non-invasive methodology based on CT imaging to quantitatively determine the relationship between the delivery parameters of the EC-ethanol formulation, its distribution, and the corresponding necrotic volume. The relationship of radiodensity to ethanol concentration was characterized with water–ethanol surrogates. Ex vivo EC-ethanol ablations were performed to optimize the formulation (n = 6). In vivo ablations were performed to compare the optimal EC-ethanol formulation to pure ethanol (n = 6). Ablations were monitored with CT and ethanol distribution volume was quantified. Livers were removed, sectioned and stained with NADH-diaphorase to determine the ablative extent, and a detailed time-course histological study was performed to assess the wound healing process. CT imaging of ethanol–water surrogates demonstrated the ethanol concentration-radiodensity relationship is approximately linear. A concentration of 12% EC in ethanol created the largest distribution volume, more than eight-fold that of pure ethanol, ex vivo. In vivo, 12% EC-ethanol was superior to pure ethanol, yielding a distribution volume three-fold greater and an ablation zone six-fold greater than pure ethanol. Finally, a time course histological evaluation of the liver post-ablation with 12% EC-ethanol and pure ethanol revealed that while both induce coagulative necrosis and similar tissue responses at 1–4 weeks post-ablation, 12% EC-ethanol yielded a larger ablation zone. The current study demonstrates the suitability of CT imaging to determine distribution volume and concentration of ethanol in tissue. The distribution volume of EC-ethanol is nearly equivalent to the resultant necrotic volume and increases distribution and necrosis compared to pure ethanol.

The impact of chronic alcohol overuse on right ventricular myocardial strain

Background The mechanisms and detail effects of alcohol cardiac toxicity are not clear. Purpose We aimed, to evaluate the relationship between the consumed alcohol dose and severity of right ventricle (RV) myocardial injury in patients overusing alcohol. Methods We collected a group of patients chronically overusing alcohol (ALC- alcohol overusers) and matched to them control group of abstainers (CG-control group). Clinical and echocardiography data have been obtained and statistical analysis performed. RV strain data were obtained from free wall (RVGS). Strain data were presented as absolute values. Results Group with available and feasible data of RV function consisted of 53 ALC patients, 75% men, 50±12 years old, and 33 controls CG, 69% men. Alcohol unit (AU – 10 gram of pure ethanol) consumed per week (AUW) was 21 (12–44) in ALC and 0 (0–0) in CG, P<0.001. The mean time of alcoholism amounted 20 (10–26) years. RVGS was: 20±7% in ALC vs. 24±3% in CG, P=0.001. In ALC, RV middle segment strain (RVmid) was 22±8% vs. 24±3%, P=0.01 and RV apical segment strain (RVapx) was 17±7 vs. 22±3, P=0.0002, see Table. No significant differences were detected for RV diameter, TAPSE and RVS', see Table. Moreover, univariate analysis showed significant positive correlation between free time (FT- time between last alcohol ingestion and echocardiography examination) and RVGS (rho = 0.36, P=0.01) as well as between FT and global longitudinal left ventricle strain (LVGS) (rho = 0.33, P=0.01), whereas TAPSE and RVS' did not show this relationship (rho = 0.30, P=0.41 and rho = 0.21, P=0.14, respectively). See Figure for RVGS. Conclusions Chronic alcohol overuse was associated with significant worsening of RV function expressed by absolute values of RVGS and RV middle and apical segment strains, offering novel quantitative parameter for reflecting early, often subclinical, impairment of RV function. RVGS and LVGS (contrary to TAPSE and RVS') reflected also myocardial function recovery after alcohol intake cessation proportionally to the elapsed abstinence time. FUNDunding Acknowledgement Type of funding sources: None. Table 1 Figure 1

Impact of a Partial Solid Solution and Water Molecules on the Formation of Fibrous Crystals and Fluid Inclusions

Resolution of (±)ibuprofen using S-α-Methylbenzylamine in pure ethanol leads to the enriched S-IBU/S-αMBA diastereomeric salt which crystallizes as very fine needles. In order to improve the filterability and processability of the solid phase, water can be added to the medium and lead to more equant particles that are still elongated. A high fraction of the resulting platelets display on both ends a fluid inclusion containing both liquid and a large bubble of gas. A detailed analysis of the particles reveals that they are not really single crystals but more an ordered association of fibers defined as fibrous crystal. A domain of partial solid solution is evidenced near the pure less soluble diastereomer and its impact on the formation of fibrous crystals is demonstrated. When pure S-IBU/S-αMBA diastereomeric salt is recrystallized in the same medium (e.g., ethanol–water) the crystallinity is improved, but fluid inclusions can still be observed.

Identification of Specific Substances in the FAIMS Spectra of Complex Mixtures Using Deep Learning

High-field asymmetric ion mobility spectrometry (FAIMS) spectra of single chemicals are easy to interpret but identifying specific chemicals within complex mixtures is difficult. This paper demonstrates that the FAIMS system can detect specific chemicals in complex mixtures. A homemade FAIMS system is used to analyze pure ethanol, ethyl acetate, acetone, 4-methyl-2-pentanone, butanone, and their mixtures in order to create datasets. An EfficientNetV2 discriminant model was constructed, and a blind test set was used to verify whether the deep-learning model is capable of the required task. The results show that the pre-trained EfficientNetV2 model completed convergence at a learning rate of 0.1 as well as 200 iterations. Specific substances in complex mixtures can be effectively identified using the trained model and the homemade FAIMS system. Accuracies of 100%, 96.7%, and 86.7% are obtained for ethanol, ethyl acetate, and acetone in the blind test set, which are much higher than conventional methods. The deep learning network provides higher accuracy than traditional FAIMS spectral analysis methods. This simplifies the FAIMS spectral analysis process and contributes to further development of FAIMS systems.

Improvement of Carrot Accelerated Solvent Extraction Efficacy Using Experimental Design and Chemometric Techniques

Human studies have demonstrated the multiple health benefits of fruits and vegetables. Due to its high fiber, mineral and antioxidant content, carrot is an ideal source for the development of nutraceuticals or functional ingredients. Current research assesses accelerated solvent extraction (ASE) traits which affect the antioxidant qualities of carrot extract using response surface methodology (RSM), hierarchical cluster analysis (HCA), and the sum of ranking differences (SRD). A mixture of organic solvents, acetone, and ethanol with or without the addition of 20% water was applied. The total carotenoid and polyphenol contents in extracts, as well as their scavenging activity and reducing power, were used as responses for the optimization of ASE extraction. RSM optimization, in the case of 20% water involvement, included 49% of acetone and 31% of ethanol (Opt1), while in the case of pure organic solvents, pure ethanol was the best choice (Opt2). The results of HCA clearly pointed out significant differences between the properties of extracts with or without water. SRD analysis confirmed ethanol to be optimal as well. RSM, HCA, and SRD analysis confirmed the same conclusion—water in the solvent mixture can significantly affect the extraction efficacy, and the optimal solvent for extracting antioxidants from carrot by ASE is pure ethanol.

Sustainable Extraction Techniques for Obtaining Antioxidant and Anti-Inflammatory Compounds from the Lamiaceae and Asteraceae Species

Melissa officinalis L. and Origanum majorana L., within Lamiaceae family, and Calendula officinalis L. and Achillea millefolium L., within the Asteraceae, have been considered a good source of bioactive ingredients with health benefits. In this study, the supercritical fluid extraction (SFE) using pure CO2, and the ultrasound assisted extraction (UAE) were proposed as green techniques to obtain plant-based extracts with potential antioxidant and anti-inflammatory activities. Higher values of total phenolic content and antioxidant activity were achieved in UAE ethanol:water (50:50, v/v) extracts. Meanwhile, UAE pure ethanol extracts showed greater anti-inflammatory activity. RP-HPLC-PAD-ESI-QTOF-MS/MS analysis showed a vast number of phenolic compounds in the extracts, including unreported ones. O. majorana ethanol:water extract presented the highest content of phenolics and antioxidant activity; among its composition, both rosmarinic acid and luteolin glucoside derivatives were abundant. The pure ethanol extract of A. millefolium resulted in an important content of caffeoylquinic acid derivatives, luteolin-7-O-glucoside and flavonoid aglycones, which could be related to the remarkable inhibition of TNF-α, IL-1β and IL-6 cytokines. Besides, borneol and camphor, found in the volatile fraction of A. millefolium, could contributed to this latter activity. Thus, this study points out that O. majorana and A. millefolium are considered a promising source of bioactive ingredients with potential use in health promotion.